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ASSOCIATION OF POLYMORPHIC VARIANTS OF FTO AND MC4R GENES WITH OBESITY IN A TATAR POPULATION
Kochetova, O.V., Korytina, G.F., Akhmadishina, L.Z., Semenov, E.E., Viktorova, T.V. (2014)
Rare Allele
МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИЙ АНАЛИЗ СЛУЧАЯ ЧАСТИЧНОЙ ДЕЛЕЦИИ Y-ХРОМОСОМЫ В СУДЕБНО-МЕДИЦИНСКОЙ ПРАКТИКЕ
MOLECULAR-GENETIC ANALYSIS OF A RARE FORENSIC CASE OF PARTIAL DELETION OF THE Y-CHROMOSOME
ТИМАШЕВА, Я.Р., ТУКТАРОВА, И.А., ГИЗУЛЛИНА, Л.И., СУНДЫРЕВ, Е.Ю., МУСТАФИНА, О.Е., Timasheva Ya.R., Tuktarova I.A., Gizullina L.I., Sundyrev E.Yu., Mustafina O.E. (2019)
MOLECULAR-GENETIC ANALYSIS OF A RARE FORENSIC CASE OF PARTIAL DELETION OF THE Y-CHROMOSOME
Role of Neurotransmitter System Genes in Chronic Obstructive Pulmonary Disease
Korytina, GF, Akhmadishina, LZ, Kochetova, OV, Nasibullin, TR, Aznabaeva, YG, Zulkarneev, SR, Izmailova, SM, Zagidullin, SZ, Victorova, TV (2021)
was significantly higher in carriers of the rare allele A of GRIK3 (rs534131A>G) and the genotype GC of GRIN2B (rs
ROLE OF NEUROTRANSMITTER SYSTEM GENES IN CHRONIC OBSTRUCTIVE PULMONARY DISEASE
KORYTINA, G.F., AKHMADISHINA, L.Z., KOCHETOVA, O.V., NASIBULLIN, T.R., AZNABAEVA, Y.G., ZULKARNEEV, S.R., IZMAǏLOVA, S.M., ZAGIDULLIN, S.Z., VICTOROVA, T.V. (2021)
was significantly higher in carriers of the rare allele A of GRIK3 (rs534131A>G) and the genotype GC of GRIN2B (rs
Evaluation of VDR and PAI allelic genes in patients with avascular necrosis of the femoral head
Volkov, E.E., Goloshchapov, A.P., Mustafin, R.N. (2021)
Objective To evaluate the informative value of the carrier status for allelic variations
Genetic variants in UNC93B1 predispose to childhood-onset systemic lupus erythematosus
Al-Azab, Mahmoud, Idiiatullina, Elina, Liu, Ziyang, Lin, Meng, Hrovat-Schaale, Katja, Xian, Huifang, Zhu, Jianheng, Yang, Mandy, Lu, Bingtai, Zhao, Zhiyao, Liu, Yiyi, Chang, Jingjie, Li, Xiaotian, Guo, Caiqin, Liu, Yunfeng, Wu, Qi, Chen, Jiazhang, Lan, Chaoting, Zeng, Ping, Cui, Jun, Gao, Xia, Zhou, Wenhao, Zhang, Yan, Zhang, Yuxia, Masters, Seth L. (2024)
Rare genetic variants in toll-like receptor 7 (TLR7) are known to cause lupus in humans and mice
Single nucleotide polymorphism rs527236194 of the cytochrome B gene (MT-CYB) is associated with alterations in sperm parameters
Gromenko, Yulia Yu., Galimov, Kamil S., Gilyazova, Irina R., Galimova, Elmira F., Bulygin, Kirill V., Ryagin, Sergey N., Galimov, Shamil N., Litvitskiy, Peter F., Piavchenko, Gennadii A., Pavlov, Valentin N. (2023)
and genotyping of polymorphic loci in the MT-CYB gene was performed using the TaqMan allelic discrimination assay
Association between miRNA Target Sites and Incidence of Primary Osteoarthritis in Women from Volga-Ural Region of Russia: A Case-Control Study
Tyurin, A, Shapovalova, D, Gantseva, H, Pavlov, V, Khusainova, R (2021)
in women from the Volga-Ural region of Russia using competitive allele-specific PCR. The T allele of the rs
ТЕРАТОМА: ТИПЫ, СИМПТОМЫ, ПРИЧИНЫ, ЛЕЧЕНИЕ
TERATOMA: TYPES, SYMPTOMS, CAUSES, TREATMENT
Аухадиева, Л.Р., Aukhadieva, L.R. (2024)
a rare tumor
Ассоциация генов CRP , CD14, провоспалительных цитокинов и их рецепторов ( TNFA , LTA , TNFRSF1A , TNFRSF1B , IL1B и IL6 ) с развитием хронической обструктивной болезни легких
ASSOCIATION OFCRP,CD14,PRO-INFLAMMATORY CYTOKINES AND THEIR RECEPTORS (TNFA, LTA, TNFRSF1A, TNFRSF1B, IL1B, AND IL6) GENES WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE DEVELOPMENT
Корытина, Г.Ф., Ахмадишина, Л.З., Кочетова, О.В., Азнабаева, Ю.Г., Измайлова, С.М., Загидуллин, Ш. З., Викторова, Т.В., KORYTINA G.F., AKHMADISHINA L. Z., KOCHETOVA O. V., AZNABAEVA Y. G., IZMAILOVA S.M., ZAGIDULLIN SH.Z., VICTOROVA T.V. (2020)

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